A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1326e214



Internal ID22757220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120876249..120945973hg38UCSC Ensembl
chr7:120516303..120586027hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3869725
hg1969725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3614811, esv3614810
SamplesHG01578
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1326e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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